Manage clinical elements of trials: site start-up, enrolment, monitoring, data cleaning, close-out.
Successful execution of assigned trials and completion of trial deliverables.
Coordinate regulatory docs and cross-functional trial oversight.
Mentoring and training of team members.
Identify risks to timelines and deliverables; propose action plans.
Lead CRAs to establish site relationships for high-quality oversight.

🎯 Requirements

Bachelor’s degree or equivalent in science/health.
Lead multi-country clinical studies in CRO/Pharma/biotech (clinical lead).
GCP/ICH knowledge and clinical development process.
Willingness to travel domestically and internationally.
English language proficiency.
MS Office, MS Project, PowerPoint; CTMS, eTMF, EDC, IXRS.

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